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FDA 510(k)

CORDIS DOW INFUSION PUMP

K-Number: K802301 · 1980-10-23

ApplicantCordis Corp.
Decision Date1980-10-23
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CORDIS DOW INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802301. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORDIS DOW INFUSION PUMP?

CORDIS DOW INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Cordis Corp.. The 510(k) number is K802301.

When did CORDIS DOW INFUSION PUMP receive FDA 510(k) clearance?

CORDIS DOW INFUSION PUMP received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802301.

Who is the listed applicant for CORDIS DOW INFUSION PUMP?

The FDA 510(k) record lists Cordis Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORDIS DOW INFUSION PUMP?

The FDA product code for CORDIS DOW INFUSION PUMP is FRN.

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Other records listing Cordis Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: FRN)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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